April 5 (Reuters) - The U.S. Food and drug
Administration on Friday allowed use of Bristol-Myers Squibb
BMY.N and 2seventybio's TSVT.O cell therapy Abecma in less
severely affected patients with a type of blood cancer.
The health regulator is also reviewing another cancer cell
therapy, Carvykti, from Johnson & Johnson JNJ.N and its
partner Legend Biotech LEGN.O for use in less severely
affected patients.
(Reporting by Sneha S K and Bhanvi Satija in Bengaluru; Editing
by Krishna Chandra Eluri)
((Sneha.SK@thomsonreuters.com;))